Condition: AUTISM, SUSCEPTIBILITY TO, 18
rs1566446604 in
CHD8 gene and
AUTISM, SUSCEPTIBILITY TO, 18
PMID 26789910 2016 A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.
PMID 24998929 2014 Disruptive CHD8 mutations define a subtype of autism early in development.
PMID 23160955 2012 Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
PMID 22495309 2012 Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.
rs1555313219 in
CHD8;SNORD9 gene and
AUTISM, SUSCEPTIBILITY TO, 18
PMID 24998929 2014 Disruptive CHD8 mutations define a subtype of autism early in development.
PMID 26789910 2016 A de novo frameshift mutation in chromodomain helicase DNA-binding domain 8 (CHD8): A case report and literature review.
PMID 23160955 2012 Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders.
PMID 22495309 2012 Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations.